Syntactx, now part of NAMSA, is a leading, full-service Clinical Research Organization (CRO) renowned for its deep expertise in complex, interventional medical device and drug trials. Clients rely on Syntactx to synthesize the clinical evidence behind their innovative products for market approvals and broad market adoption, leveraging its team of seasoned clinical and regulatory professionals. Syntactx is committed to providing comprehensive solutions across various domains.
With a technology-driven approach, Syntactx has successfully enrolled over 200,000 subjects in North America, Europe, and Asia since 2010. Headquartered at 4 World Trade Center, 150 Greenwich Street, 44th Floor, New York, NY 10006, US, Syntactx also maintains a presence at Tolstraat 26, Herzele, Belgium 9550, BE, and 8 Shenton Way, #05-02, AXA Tower, Singapore, 068811, SG. The company offers expert guidance through strategy and consulting, clinical operations, regulatory affairs, data sciences, safety, imaging core laboratory, and medical writing.
Syntactx, now part of NAMSA, is dedicated to helping clients improve the lives of patients worldwide. The company’s offerings include site selection, post-market studies, BIMO audits, electronic data capture, SAS programming, medical writing, and regulatory submissions. Information about the company is being completed soon with the support of Syntactx management. We invite the company’s manager to create a customized and exclusive company showcase and product listing on our platform.
Compare Syntactx, Now Part of NAMSA with 3 companies in Research-Services
| Comparison Field |
Syntactx, Now Part of NAM...Main Company |
VeristatView Profile |
Fu
Future Technologies...View Profile |
AHL WaterView Profile |
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Founded Year
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— | 2021 | 2016 | |
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Company Size
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— | 501-1,000 | 2-10 | 11-50 |
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City
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New York, NY | Southborough, Massachusetts | Basra, Basra | City of Tshwane, Gauteng |
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Country
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United States | Iraq | South Africa | |
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Skills & Keywords
Comparing with main company
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28 Total Skills
Clinical Research Organization
Medical Device Trials
Drug Trials
Regulatory Affairs
Clinical Operations
Data Sciences
Medical Writing
Site Selection
Safety
Post Market Studies
BIMO Audit
Electronic Data Capture
Management
SAS Programming
Medical & Combination Devices
Contracting
PMA Submissions
FDA Panel Prep
Clinical Evaluation Reports
Investigator-Initiated Research
Data Analysis & Statistics
Imaging Core Laboratory
Site Monitoring
CEC & DSMB Oversight
Pharmaceuticals
Regulatory Submissions
Trial Design
Global Regulatory Strategy
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21 Total
21 Unique
Unique Skills:
Adaptive Clinical Trial Design
Biologic
Biostatistics
Clinical Trial Data Standardization
Clinical Trial Management
Clinical Trial Patient Recruitment
+15
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24 Total
24 Unique
Unique Skills:
Crane Safety
Development
Environment
First Aid
Health
HR
+18
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10 Total
10 Unique
Unique Skills:
Compliance
Consulting
Delivery
Environment
Innovation
Reliability
+4
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